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Signal Transduction Signaling Pathway G Protein Signaling Small G Proteins Other

PX-866, PI3-kinase inhibitor (ab142172)

Key features and details

  • Potent, irreversible PI3-kinase inhibitor
  • CAS Number: 502632-66-8
  • Purity: > 98%
  • Soluble in DMSO to 50 mM
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    PX-866, PI3-kinase inhibitor
  • Description

    Potent, irreversible PI3-kinase inhibitor
  • Alternative names

    • DJM-166
    • DJM-2-166
    • Sonolisib
  • Biological description

    Potent, irreversible PI3-kinase inhibitor. Inhibits purified phosphoinositide (PtdIns)-3-kinase (IC50 = 0.1 nM) and PtdIns-3-kinase signaling as assessed by phospho-Ser473-Akt levels in HT-29 colon cancer cells (IC50 = 20 nM). Ring-opened analog of wortmannin (ab120148). Displays antitumor activity.

  • Purity

    > 98%
  • CAS Number

    502632-66-8
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    [(3aR,6E,9S,9aR,10R,11aS)-6-[[Bis(prop-2-enyl)amino]methylidene]-5-hydroxy-9-(methoxymethyl)-9a,11a-dimethyl-1,4,7-trioxo-2,3,3a,9,10,11-hexahydroindeno[4,5-h]isochromen-10-yl] acetate
  • Molecular weight

    525.59
  • Molecular formula

    C29H35NO8
  • PubChem identifier

    9849735
  • Storage instructions

    Shipped at Room Temperature. Store at -20°C. Store under desiccating conditions.
  • Solubility overview

    Soluble in DMSO to 50 mM
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    CC(=O)O[C@@H]1C[C@]2([C@@H](CCC2=O)C3=C1[C@]4([C@H](OC(=O)/C(=C/N(CC=C)CC=C)/C4=C(C3=O)O)COC)C)C
  • Source

    Synthetic

  • Research areas

    • Cell Biology
    • Cell Cycle
    • Cell Cycle Inhibitors
    • Other
    • Epigenetics and Nuclear Signaling
    • DNA / RNA
    • DNA Damage & Repair
    • DNA Damage Response
    • DNA Damage Recognition
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • PKA
    • Signal Transduction
    • Signaling Pathway
    • Lipid Signaling
    • Lipid Kinases
    • Cancer
    • Cell cycle
    • Cell cycle inhibitors
    • Other
    • Cancer
    • Signal transduction
    • Other
    • Cancer
    • Oncoproteins/suppressors
    • Oncoproteins
    • Signal transducers
    • Cardiovascular
    • Heart
    • Cardiogenesis
    • Transcription factors/regulators
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    • Innate Immunity
    • TLR Signaling
    • Cancer
    • Cancer Metabolism
    • Metabolic signaling pathway
    • Metabolism of lipids and lipoproteins
    • Cancer
    • Cancer Metabolism
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    • Integration of energy metabolism
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    • Energy transfer pathways
    • Integration of energy
    • Metabolism
    • Types of disease
    • Obesity

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